Roman Sanziana
Yale University School of Medicine, New Haven, CT 06520, USA.
Curr Opin Oncol. 2004 Jan;16(1):8-12. doi: 10.1097/00001622-200401000-00003.
Pheochromocytomas and paragangliomas are rare tumors of chromaffin cell origin. Their identification is likely increasing owing to the increased use of radiographic images detecting incidental adrenal masses.
The pathophysiology of hypertension induced by the release of catecholamines and newly discovered peptides has been shown to be more complex than the concept of episodic catecholamine release.
This review looks at the most recent advances in the physiology and molecular basis of these tumors.